Canonical Allele Identifier: CA2670356520

Gene: WDR19

Linked Data

• gnomAD v4: 4-39206029-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39206029T>A , CM000666.2:g.39206029T>A	GRCh38
NC_000004.11:g.39207649T>A , CM000666.1:g.39207649T>A	GRCh37
NC_000004.10:g.38884044T>A	NCBI36
NG_031813.1:g.28626T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.890+293T>A MANE Select	ENSP00000382717.3:n.890+293T>A
ENST00000399820.7:c.890+293T>A	ENSP00000382717.3:n.890+293T>A
ENST00000503697.5:c.*358+293T>A	ENSP00000423706.1:n.*358+293T>A
ENST00000506503.1:c.890+293T>A	ENSP00000423491.1:n.890+293T>A
ENST00000506869.5:c.*471+293T>A	ENSP00000424319.1:n.*471+293T>A
ENST00000511729.5:n.41-22529T>A
ENST00000512448.1:n.777T>A
NM_025132.3:c.890+293T>A	NP_079408.3:n.890+293T>A
XM_011513724.1:c.890+293T>A	XP_011512026.1:n.890+293T>A
XM_011513725.1:c.824+293T>A	XP_011512027.1:n.824+293T>A
XM_011513726.1:c.410+293T>A	XP_011512028.1:n.410+293T>A
XM_011513727.1:c.410+293T>A	XP_011512029.1:n.410+293T>A
XM_011513728.1:c.410+293T>A	XP_011512030.1:n.410+293T>A
XM_011513729.1:c.890+293T>A	XP_011512031.1:n.890+293T>A
XR_925155.1:n.954+293T>A
NM_001317924.1:c.410+293T>A	NP_001304853.1:n.410+293T>A
XM_011513725.2:c.824+293T>A	XP_011512027.1:n.824+293T>A
XM_011513726.3:c.410+293T>A	XP_011512028.1:n.410+293T>A
XM_017008501.1:c.410+293T>A	XP_016863990.1:n.410+293T>A
XR_001741306.1:n.954+293T>A
XR_001741307.1:n.954+293T>A
XR_001741308.1:n.954+293T>A
XR_001741309.1:n.954+293T>A
XR_001741310.1:n.954+293T>A
XR_001741311.2:n.803+293T>A
XR_001741312.1:n.954+293T>A
NM_025132.4:c.890+293T>A MANE Select	NP_079408.3:n.890+293T>A
NM_001317924.2:c.410+293T>A	NP_001304853.1:n.410+293T>A